Canonical Allele Identifier: CA456752879
Gene: ACTL6B HGNC NCBI

Linked Data

dbSNP Id: rs2131333274
MyVariant Identifiers: chr7:g.100244222C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100646599C>T , CM000669.2:g.100646599C>T GRCh38
NC_000007.13:g.100244222C>T , CM000669.1:g.100244222C>T GRCh37
NC_000007.12:g.100082158C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000160382.10:c.1065G>A MANE Select ENSP00000160382.5:p.Gln355=
ENST00000160382.9:c.1065G>A ENSP00000160382.5:p.Gln355=
ENST00000487125.1:n.627G>A
NM_016188.4:c.1065G>A NP_057272.1:p.Gln355=
XR_927476.1:n.1172G>A
NR_134539.1:n.1172G>A
NM_016188.5:c.1065G>A MANE Select NP_057272.1:p.Gln355=
NR_134539.2:n.1159G>A
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